OA11654A - N-alkylaspartyldipeptide ester derivatives and sweeteners. - Google Patents

N-alkylaspartyldipeptide ester derivatives and sweeteners. Download PDF

Info

Publication number: OA11654A
Authority: OA; OAPI
Prior art keywords: group; dénotés; dénoté; dérivative; hydrogen atom
Prior art date: 1998-09-18

Application number

OA1200100069A

Other languages

English (en)

Inventor

Yusuke Amino

Kazuko Yuzawa

Tadashi Takemoto

Ryoichiro Nakamura

Original Assignee

Ajinomoto Kk

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1998-09-18

Filing date

1999-09-10

Publication date

2004-12-08

1999-09-10 Application filed by Ajinomoto Kk filed Critical Ajinomoto Kk

2004-12-08 Publication of OA11654A publication Critical patent/OA11654A/en

Links

235000003599 food sweetener Nutrition 0.000 title claims abstract description 21
239000003765 sweetening agent Substances 0.000 title claims abstract description 21
150000002148 esters Chemical class 0.000 title claims abstract description 14
235000013305 food Nutrition 0.000 claims abstract description 9
108010016626 Dipeptides Proteins 0.000 claims abstract description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 76
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 65
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 49
125000004432 carbon atom Chemical group C* 0.000 claims description 42
125000001424 substituent group Chemical group 0.000 claims description 42
-1 hydroxvl group Chemical group 0.000 claims description 36
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 32
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 26
125000000217 alkyl group Chemical group 0.000 claims description 20
125000004429 atom Chemical group 0.000 claims description 20
125000002947 alkylene group Chemical group 0.000 claims description 10
229910052799 carbon Inorganic materials 0.000 claims description 9
125000003143 4-hydroxybenzyl group Chemical group [H]C([*])([H])C1=C([H])C([H])=C(O[H])C([H])=C1[H] 0.000 claims description 8
125000003545 alkoxy group Chemical group 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 5
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 3
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 2
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 2
SGPGESCZOCHFCL-UHFFFAOYSA-N Tilisolol hydrochloride Chemical compound [Cl-].C1=CC=C2C(=O)N(C)C=C(OCC(O)C[NH2+]C(C)(C)C)C2=C1 SGPGESCZOCHFCL-UHFFFAOYSA-N 0.000 claims 4
125000001874 trioxidanyl group Chemical group [*]OOO[H] 0.000 claims 1
235000010357 aspartame Nutrition 0.000 abstract description 77
FGOJCPKOOGIRPA-UHFFFAOYSA-N 1-o-tert-butyl 4-o-ethyl 5-oxoazepane-1,4-dicarboxylate Chemical compound CCOC(=O)C1CCN(C(=O)OC(C)(C)C)CCC1=O FGOJCPKOOGIRPA-UHFFFAOYSA-N 0.000 abstract description 58
229960005190 phenylalanine Drugs 0.000 abstract description 57
150000003839 salts Chemical group 0.000 abstract description 9
150000001875 compounds Chemical class 0.000 description 50
230000015572 biosynthetic process Effects 0.000 description 24
238000003786 synthesis reaction Methods 0.000 description 24
IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 22
238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 22
108010011485 Aspartame Proteins 0.000 description 15
IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical group OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 15
239000000605 aspartame Substances 0.000 description 15
229960003438 aspartame Drugs 0.000 description 15
239000000126 substance Substances 0.000 description 15
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 13
238000000034 method Methods 0.000 description 13
239000000047 product Substances 0.000 description 11
239000007787 solid Substances 0.000 description 11
239000005720 sucrose Substances 0.000 description 11
229960004793 sucrose Drugs 0.000 description 11
229930006000 Sucrose Natural products 0.000 description 10
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 10
238000005932 reductive alkylation reaction Methods 0.000 description 10
230000002829 reductive effect Effects 0.000 description 10
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
239000000243 solution Substances 0.000 description 8
YGCZTXZTJXYWCO-UHFFFAOYSA-N 3-phenylpropanal Chemical compound O=CCCC1=CC=CC=C1 YGCZTXZTJXYWCO-UHFFFAOYSA-N 0.000 description 6
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
239000001257 hydrogen Substances 0.000 description 6
229910052739 hydrogen Inorganic materials 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 5
150000001721 carbon Chemical group 0.000 description 5
239000000706 filtrate Substances 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 4
WKJCDFFFNKELIP-UHFFFAOYSA-N 3-(3-methoxy-4-phenylmethoxyphenyl)but-2-enal Chemical compound COC1=CC(C(C)=CC=O)=CC=C1OCC1=CC=CC=C1 WKJCDFFFNKELIP-UHFFFAOYSA-N 0.000 description 4
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
VSDUZFOSJDMAFZ-VIFPVBQESA-N methyl L-phenylalaninate Chemical group COC(=O)[C@@H](N)CC1=CC=CC=C1 VSDUZFOSJDMAFZ-VIFPVBQESA-N 0.000 description 4
229920006395 saturated elastomer Polymers 0.000 description 4
235000019605 sweet taste sensations Nutrition 0.000 description 4
229960004441 tyrosine Drugs 0.000 description 4
241000790917 Dioxys <bee> Species 0.000 description 3
COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 3
229940024606 amino acid Drugs 0.000 description 3
235000001014 amino acid Nutrition 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
239000003638 chemical reducing agent Substances 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
238000000605 extraction Methods 0.000 description 3
239000007788 liquid Substances 0.000 description 3
UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 3
239000000203 mixture Substances 0.000 description 3
230000001953 sensory effect Effects 0.000 description 3
238000004809 thin layer chromatography Methods 0.000 description 3
NYNZQNWKBKUAII-KBXCAEBGSA-N (3s)-n-[5-[(2r)-2-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrazolo[1,5-a]pyrimidin-3-yl]-3-hydroxypyrrolidine-1-carboxamide Chemical compound C1[C@@H](O)CCN1C(=O)NC1=C2N=C(N3[C@H](CCC3)C=3C(=CC=C(F)C=3)F)C=CN2N=C1 NYNZQNWKBKUAII-KBXCAEBGSA-N 0.000 description 2
GWYCJXDHVRQZKQ-UHFFFAOYSA-N 3-(4-methoxy-3-phenylmethoxyphenyl)but-2-enal Chemical compound COC1=CC=C(C(C)=CC=O)C=C1OCC1=CC=CC=C1 GWYCJXDHVRQZKQ-UHFFFAOYSA-N 0.000 description 2
KJPRLNWUNMBNBZ-UHFFFAOYSA-N 3-phenylprop-2-enal Chemical compound O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 2
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 2
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
235000003704 aspartic acid Nutrition 0.000 description 2
OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 2
235000013361 beverage Nutrition 0.000 description 2
239000000872 buffer Substances 0.000 description 2
239000004067 bulking agent Substances 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000003814 drug Substances 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
RBAUAHIPDXKQJI-QMMMGPOBSA-N methyl (2s)-2-anilinopropanoate Chemical compound COC(=O)[C@H](C)NC1=CC=CC=C1 RBAUAHIPDXKQJI-QMMMGPOBSA-N 0.000 description 2
239000012046 mixed solvent Substances 0.000 description 2
HLIAVLHNDJUHFG-UHFFFAOYSA-N neotame Chemical compound CC(C)(C)CCNC(CC(O)=O)C(=O)NC(C(=O)OC)CC1=CC=CC=C1 HLIAVLHNDJUHFG-UHFFFAOYSA-N 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
239000012044 organic layer Substances 0.000 description 2
108090000765 processed proteins & peptides Proteins 0.000 description 2
125000006239 protecting group Chemical group 0.000 description 2
JRWPBBXPNLJFMJ-VQHVLOKHSA-N (e)-3-(4-methoxyphenyl)but-2-enal Chemical compound COC1=CC=C(C(\C)=C\C=O)C=C1 JRWPBBXPNLJFMJ-VQHVLOKHSA-N 0.000 description 1
IYSCWHOEHVUWPT-UHFFFAOYSA-N 3-(3-methyl-4-phenylmethoxyphenyl)but-2-enal Chemical compound CC1=CC(C(=CC=O)C)=CC=C1OCC1=CC=CC=C1 IYSCWHOEHVUWPT-UHFFFAOYSA-N 0.000 description 1
ZUUYNMHGDXJJDW-UHFFFAOYSA-N 3-(3-phenylmethoxyphenyl)but-2-enal Chemical compound O=CC=C(C)C1=CC=CC(OCC=2C=CC=CC=2)=C1 ZUUYNMHGDXJJDW-UHFFFAOYSA-N 0.000 description 1
HLUHNUTVLIMUGY-UHFFFAOYSA-N 3-(4-methoxy-3-phenylmethoxyphenyl)-2-methylprop-2-enal Chemical compound COC1=CC=C(C=C(C)C=O)C=C1OCC1=CC=CC=C1 HLUHNUTVLIMUGY-UHFFFAOYSA-N 0.000 description 1
125000006201 3-phenylpropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
239000004475 Arginine Substances 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
101001081176 Homo sapiens Hyaluronan mediated motility receptor Proteins 0.000 description 1
102100027735 Hyaluronan mediated motility receptor Human genes 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
VTAJIXDZFCRWBR-UHFFFAOYSA-N Licoricesaponin B2 Natural products C1C(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2)C(O)=O)C)(C)CC2)(C)C2C(C)(C)CC1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O VTAJIXDZFCRWBR-UHFFFAOYSA-N 0.000 description 1
KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
239000004472 Lysine Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
YGCFIWIQZPHFLU-UHFFFAOYSA-N acesulfame Chemical compound CC1=CC(=O)NS(=O)(=O)O1 YGCFIWIQZPHFLU-UHFFFAOYSA-N 0.000 description 1
229960005164 acesulfame Drugs 0.000 description 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
235000015218 chewing gum Nutrition 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
239000000625 cyclamic acid and its Na and Ca salt Substances 0.000 description 1
HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 1
230000035622 drinking Effects 0.000 description 1
235000006694 eating habits Nutrition 0.000 description 1
230000000694 effects Effects 0.000 description 1
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000001914 filtration Methods 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 description 1
239000001685 glycyrrhizic acid Substances 0.000 description 1
229960004949 glycyrrhizic acid Drugs 0.000 description 1
UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 description 1
235000019410 glycyrrhizin Nutrition 0.000 description 1
LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 description 1
238000011835 investigation Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000010410 layer Substances 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
125000006237 oxymethylenoxy group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
238000010647 peptide synthesis reaction Methods 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
235000019204 saccharin Nutrition 0.000 description 1
229940081974 saccharin Drugs 0.000 description 1
239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
238000009738 saturating Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06104—Dipeptides with the first amino acid being acidic
- C07K5/06113—Asp- or Asn-amino acid
- C07K5/06121—Asp- or Asn-amino acid the second amino acid being aromatic or cycloaliphatic
- C07K5/0613—Aspartame
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
- A23L27/31—Artificial sweetening agents containing amino acids, nucleotides, peptides or derivatives
- A23L27/32—Artificial sweetening agents containing amino acids, nucleotides, peptides or derivatives containing dipeptides or derivatives

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Biochemistry (AREA)
Medicinal Chemistry (AREA)
Molecular Biology (AREA)
Genetics & Genomics (AREA)
Biophysics (AREA)
General Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Food Science & Technology (AREA)
Polymers & Plastics (AREA)
Nutrition Science (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Peptides Or Proteins (AREA)
Seasonings (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

OA1200100069A 1998-09-18 1999-09-10 N-alkylaspartyldipeptide ester derivatives and sweeteners. OA11654A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP26425298		1998-09-18
JP16941999		1999-06-16

Publications (1)

Publication Number	Publication Date
OA11654A true OA11654A (en)	2004-12-08

Family

ID=26492759

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
OA1200100069A OA11654A (en)	1998-09-18	1999-09-10	N-alkylaspartyldipeptide ester derivatives and sweeteners.

Country Status (22)

Country	Link
US (1)	US7238830B2 (es)
EP (1)	EP1114828B1 (es)
KR (1)	KR100601746B1 (es)
CN (1)	CN1206238C (es)
AR (1)	AR023048A1 (es)
AT (1)	ATE388959T1 (es)
AU (1)	AU748136B2 (es)
BR (1)	BR9913779B1 (es)
CA (1)	CA2344314A1 (es)
CZ (1)	CZ2001974A3 (es)
DE (1)	DE69938352T2 (es)
HU (1)	HUP0103979A3 (es)
IL (1)	IL141525A0 (es)
NO (1)	NO20011156L (es)
NZ (1)	NZ510439A (es)
OA (1)	OA11654A (es)
PL (1)	PL346665A1 (es)
RU (1)	RU2207344C2 (es)
SK (1)	SK3682001A3 (es)
TR (1)	TR200100778T2 (es)
TW (1)	TW589324B (es)
WO (1)	WO2000017230A1 (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2001018034A1 (fr)	1999-09-07	2001-03-15	Ajinomoto Co., Inc.	Procede de production de derive d'aspartame, procede de purification de ce derive, cristaux et utilisation de ce derive
JP2001097998A (ja) *	1999-10-01	2001-04-10	Ajinomoto Co Inc	アスパルチルジペプチドエステル誘導体及び甘味剤
CN1378559A (zh) *	1999-10-07	2002-11-06	味之素株式会社	天冬氨酰基缩二氨酸酯衍生物的制备方法、及其新型制备中间体及该中间体的制备方法
EP1227104A4 (en)	1999-10-07	2003-04-09	Ajinomoto Kk	METHOD FOR PRODUCING ASPARTAM DERIVATIVES AND METHOD FOR PRODUCING ITS PREPARATIONS
CN1566141A (zh) *	1999-10-08	2005-01-19	味之素株式会社	天冬甜素衍生物的制造方法、其结晶体、及其新型制造中间体和该中间体的制造方法
JP2001199930A (ja)	2000-01-20	2001-07-24	Ajinomoto Co Inc	新規アリ−ルプロピルアルデヒド誘導体、その製造法及びその使用等
CA2437655A1 (en) *	2001-02-08	2002-08-15	Ajinomoto Co., Inc.	Novel n-alkylaspartyl amide derivative and sweetening agent
IN2015CH02019A (es) *	2015-04-20	2015-06-05	Divis Lab Ltd

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Publication number	Priority date	Publication date	Assignee	Title
US3475403A (en) *	1967-01-20	1969-10-28	Searle & Co	Aspartic acid containing dipeptide lower alkyl esters
FR2533210A1 (fr) *	1982-09-17	1984-03-23	Lyon I Universite Claude	Edulcorants de synthese
US4766246A (en)	1986-08-19	1988-08-23	General Foods Corporation	L-aminodicarboxylic acid esters
FR2697844B1 (fr) *	1992-11-12	1995-01-27	Claude Nofre	Nouveaux composés dérivés de dipeptides ou d'analogues dipeptidiques utiles comme agents édulcorants, leur procédé de préparation.
JP3648784B2 (ja) *	1994-07-08	2005-05-18	味の素株式会社	新規アスパルチルジペプチド誘導体及び甘味剤
JPH09323966A (ja) *	1996-01-12	1997-12-16	Ajinomoto Co Inc	新規アスパルチルアミド誘導体及び甘味剤
JP3951342B2 (ja) *	1996-07-10	2007-08-01	味の素株式会社	新規アスパルチルジペプチドアミド誘導体及び甘味剤
JPH10259194A (ja)	1997-03-18	1998-09-29	Ajinomoto Co Inc	新規ジペプチド誘導体及び甘味剤
JP3959964B2 (ja) *	1998-04-09	2007-08-15	味の素株式会社	アスパルチルジペプチドエステル誘導体及び甘味剤
JP2001097998A (ja)	1999-10-01	2001-04-10	Ajinomoto Co Inc	アスパルチルジペプチドエステル誘導体及び甘味剤

1999
- 1999-09-10 TR TR2001/00778T patent/TR200100778T2/xx unknown
- 1999-09-10 WO PCT/JP1999/004977 patent/WO2000017230A1/ja active IP Right Grant
- 1999-09-10 CZ CZ2001974A patent/CZ2001974A3/cs unknown
- 1999-09-10 IL IL14152599A patent/IL141525A0/xx unknown
- 1999-09-10 KR KR1020017003420A patent/KR100601746B1/ko not_active IP Right Cessation
- 1999-09-10 SK SK368-2001A patent/SK3682001A3/sk unknown
- 1999-09-10 NZ NZ510439A patent/NZ510439A/xx unknown
- 1999-09-10 RU RU2001111037/04A patent/RU2207344C2/ru not_active IP Right Cessation
- 1999-09-10 AU AU56501/99A patent/AU748136B2/en not_active Ceased
- 1999-09-10 EP EP99943302A patent/EP1114828B1/en not_active Expired - Lifetime
- 1999-09-10 HU HU0103979A patent/HUP0103979A3/hu unknown
- 1999-09-10 PL PL99346665A patent/PL346665A1/xx not_active Application Discontinuation
- 1999-09-10 CA CA002344314A patent/CA2344314A1/en not_active Abandoned
- 1999-09-10 OA OA1200100069A patent/OA11654A/en unknown
- 1999-09-10 BR BRPI9913779-8A patent/BR9913779B1/pt not_active IP Right Cessation
- 1999-09-10 CN CNB998104671A patent/CN1206238C/zh not_active Expired - Fee Related
- 1999-09-10 DE DE69938352T patent/DE69938352T2/de not_active Expired - Lifetime
- 1999-09-10 AT AT99943302T patent/ATE388959T1/de not_active IP Right Cessation
- 1999-09-14 TW TW088115846A patent/TW589324B/zh not_active IP Right Cessation
- 1999-09-17 AR ARP990104691A patent/AR023048A1/es unknown
2001
- 2001-03-07 NO NO20011156A patent/NO20011156L/no unknown
- 2001-03-16 US US09/809,197 patent/US7238830B2/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
CN1315959A (zh)	2001-10-03
BR9913779A (pt)	2001-07-10
CA2344314A1 (en)	2000-03-30
KR20010075156A (ko)	2001-08-09
HUP0103979A3 (en)	2003-05-28
CZ2001974A3 (cs)	2001-08-15
IL141525A0 (en)	2002-03-10
WO2000017230A1 (fr)	2000-03-30
TW589324B (en)	2004-06-01
AU5650199A (en)	2000-04-10
NO20011156L (no)	2001-05-09
EP1114828B1 (en)	2008-03-12
SK3682001A3 (en)	2001-10-08
PL346665A1 (en)	2002-02-25
CN1206238C (zh)	2005-06-15
RU2207344C2 (ru)	2003-06-27
EP1114828A4 (en)	2004-05-26
AR023048A1 (es)	2002-09-04
US20010039357A1 (en)	2001-11-08
AU748136B2 (en)	2002-05-30
TR200100778T2 (tr)	2001-07-23
KR100601746B1 (ko)	2006-07-20
BR9913779B1 (pt)	2012-01-24
NZ510439A (en)	2002-09-27
HUP0103979A2 (hu)	2002-02-28
US7238830B2 (en)	2007-07-03
EP1114828A1 (en)	2001-07-11
DE69938352D1 (de)	2008-04-24
ATE388959T1 (de)	2008-03-15
DE69938352T2 (de)	2009-03-26
NO20011156D0 (no)	2001-03-07

Publication	Publication Date	Title
RU2107071C1 (ru)	1998-03-20	Производные аспартама или их физиологически приемлемые соли, способ их получения, подслащивающее средство
JP3959964B2 (ja)	2007-08-15	アスパルチルジペプチドエステル誘導体及び甘味剤
AU752473B2 (en)	2002-09-19	Novel aspartyl dipeptide ester derivatives and sweeteners
OA11654A (en)	2004-12-08	N-alkylaspartyldipeptide ester derivatives and sweeteners.
US6649784B2 (en)	2003-11-18	Aspartyl dipeptide ester derivatives and sweeteners
MXPA01002402A (es)	2003-02-17	Derivado dipeptido ester de n-alquilaspartilo y agente edulcorante
MXPA00012122A (es)	2002-06-05	Derivados y edulcorantes de ester dipeptido de aspartilo novedosos
MXPA00009449A (es)	2001-07-09	Edulcorantes y derivados de ester dipeptido aspartilo
JP2001322996A (ja)	2001-11-20	新規ｎ−アルキルアスパルチルジペプチドエステル誘導体及び甘味剤
UA71926C2 (en)	2005-01-17	N-alkylaspartyldipeptide ester derivative and sweetening agent